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AIM ImmunoTech Releases Virtual Investor “What This Means Segment”

Key Takeaway: AIM ImmunoTech has announced the approval from the Erasmus MC Safety Committee to advance to Phase 2 of the DURIPANC clinical trial. The trial investigates the effectiveness of AIM's Ampligen® combined with AstraZeneca's Imfinzi® for treating late-stage pancreatic cancer. AIM's CEO, Tom Equels, and Prof. Casper van Eijck discussed the trial's potential in a recent virtual investor segment. The Phase 1 study's safety data indicated that the treatment combination is generally well-tolerated, showing promise for patient outcomes.

Market Sentiment Analysis

POSITIVE FACTORS

  • Approval from the Erasmus MC Safety Committee to proceed to Phase 2 study.
  • Combination treatment of Ampligen® and Imfinzi® was found generally well-tolerated.
  • No treatment-related severe adverse events or dose-limiting toxicities reported.

Full Press Release Details

Tom Equels, CEO of AIM ImmunoTech and Professor Casper H.J. van Eijck, MD, PhD, Pancreato-biliary Surgeon at Erasmus MC, discuss the Phase 1b/2 clinical trial involving AIM’s Ampligen® (rintatolimod) and AstraZeneca’s anti-PD-L1 immune checkpoint inhibitor Imfinzi® (durvalumab) in the treatment of late-stage pancreatic cancer (“DURIPANC”)
Watch the “What This Means” segment here
OCALA, Fla., Feb. 11, 2025 (GLOBE NEWSWIRE) -- AIM ImmunoTech Inc. (NYSE American: AIM) (“AIM” or the “Company”) today announced that AIM CEO Thomas K. Equels and Prof. Casper H.J. van Eijck, MD, PhD, Pancreato-biliary Surgeon at the Erasmus Medical Center (“Erasmus MC”) and Coordinating Investigator for the DURIPANC study in late-stage pancreatic cancer, participated in a Virtual Investor “What This Means” segment. Access the segment here.
As part of the segment, Mr. Equels and Professor van Eijck discuss the recent approval from the Erasmus MC Safety Committee to proceed with the Phase 2 Study of Ampligen® and AstraZeneca’s Imfinzi as a potential combination treatment for late-stage pancreatic cancer. DURIPANC is an investigator-initiated, exploratory, open-label, single-center study in the Netherlands at Erasmus MC. The approval to proceed to Phase 2 was granted following the Safety Committee’s review of the complete Phase 1 safety data, which found the combination treatment to be generally well-tolerated with no treatment-related severe adverse events or dose-limiting toxicities.
The Virtual Investor “What this Means” segment featuring AIM ImmunoTech is now available here.
About AIM ImmunoTech Inc.
AIM ImmunoTech Inc. is an immuno-pharma company focused on the research and development of therapeutics to treat multiple types of cancers, immune disorders and viral diseases, including COVID-19. The Company’s lead product is a first-in-class investigational drug called Ampligen® (rintatolimod), a dsRNA and highly selective TLR3 agonist immuno-modulator with broad spectrum activity in clinical trials for globally important cancers, viral diseases and disorders of the immune system.
For more information, please visit aimimmuno.com and connect with the Company on X, LinkedIn, and Facebook.
Cautionary Statement
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 (the “PSLRA”). Words such as “may,” “will,” “expect,” “plan,” “anticipate,” “continue,” “believe,” “potential,” “upcoming” and other variations thereon and similar expressions (as well as other words or expressions referencing future events or circumstances) are intended to identify forward-looking statements. Many of these forward-looking statements involve a number of risks and uncertainties. Data, pre-clinical success and clinical success seen to date do not guarantee that Ampligen will be approved as a therapy for pancreatic cancer. The Company urges investors to consider specifically the various risk factors identified in its most recent Form 10-K, and any risk factors or cautionary statements included in any subsequent Form 10-Q or Form 8-K, filed with the U.S. Securities and Exchange Commission. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this press release. Among other things, for those statements, the Company claims the protection of the safe harbor for forward-looking statements contained in the PSLRA. The Company does not undertake to update any of these forward-looking statements to reflect events or circumstances that occur after the date hereof.

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Frequently Asked Questions

What is the DURIPANC study about?

The DURIPANC study investigates the combination of Ampligen® and Imfinzi® for late-stage pancreatic cancer.

Who are the key figures in the DURIPANC study?

Tom Equels, CEO of AIM ImmunoTech, and Professor Casper H.J. van Eijck lead the study.

What was the outcome of the Phase 1 safety data?

The Phase 1 safety data showed that the combination treatment was well-tolerated.

Where is the DURIPANC study being conducted?

The study is being conducted at Erasmus MC in the Netherlands.

What is Ampligen®?

Ampligen® is an investigational drug that acts as a TLR3 agonist immuno-modulator.

Last updated: Feb 11, 2025